Lower riskFood recall · FDA · Published April 14, 2021
Jose Madrid Strawberry Mild Salsa Recall: Undeclared Anchovy Allergen
Jose Madrid recalls 13oz glass jars of Strawberry Mild Salsa due to undeclared anchovy allergen. Consumers should check product codes and contact the company for details.
“Jose Madrid Strawberry Mild Salsa Recall: Undeclared Anchovy Allergen.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14695-jose-madrid-strawberry-mild-salsa-recall-undeclared-anchovy-allergen. Based on FDA recall #F-0473-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0473-2021%22&limit=1).
The FDA announced on April 14, 2021, that Michael Zakany LLC is recalling Jose Madrid Salsa - Strawberry Mild Salsa due to an undeclared anchovy allergen. The firm initiated the voluntary recall of 6,659 jars distributed in Ohio and online across the U.S.
How to tell if you have it
Brand: Jose Madrid
Product: Jose Madrid Salsa - Strawberry Mild Salsa
Size: 13oz glass jars
Packaging: 12 jars per case
Facility Code: 601
Product Code: 19
Batch Code: 01
Serial Number: 6011901 032924
Best By Date: 03/26/20 - 03/29/24
The hazard
The product contains an undeclared anchovy allergen, which poses a risk to individuals with fish allergies. The recall is classified as a Class II hazard.
Context
GovInfoNow's records show Michael Zakany LLC has 3 other recalls on record since 2015-02-17. On 2024-11-20, Jose Madrid Salsa Chipotle Con Queso was recalled for undeclared yellow dyes. Other recent recalls of similar products include Jaime's Foods Jalapeno Ranch Recall (2026-08-05), D'Dioses Guayaba Ice Pop Recall (2026-05-04), and Sendero Gorditas de Azucar Recall (2026-03-06).
How to tell if you have this one
Check for 13oz glass jars labeled 'Jose Madrid Strawberry Mild Salsa' with product code 19, batch code 01, and serial number 6011901 032924. The best by date ranges from 03/26/20 to 03/29/24.
Brand
Jose Madrid
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the product code 19, batch code 01, and serial number 6011901 032924 on the jar's label.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Product is sold at local farmer's markets, 12 retail locations within Ohio, 1 distributor in Ohio, and online sales across the US. Estimate on sales: 1,099 jars sold through websites, 800 sold through local fundraisers, 400 sold at…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 49 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0473-2021 (April 14, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0473-2021 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.